Verma Ashutosh, Hellwage Jens, Artiushin Sergey, Zipfel Peter F, Kraiczy Peter, Timoney John F, Stevenson Brian
Gluck Equine Research Center, University of Kentucky, Lexington, KY 40546, USA.
Infect Immun. 2006 May;74(5):2659-66. doi: 10.1128/IAI.74.5.2659-2666.2006.
The early phase of leptospiral infection is characterized by the presence of live organisms in the blood. Pathogenic Leptospira interrogans is resistant to the alternative pathway of complement mediated-killing, while nonpathogenic members of the genus are not. Consistent with that observation, only pathogenic leptospires bound factor H, a host fluid-phase regulator of the alternative complement pathway. Ligand affinity blot analyses revealed that pathogenic L. interrogans produces at least two factor H-binding proteins. Through screening of a lambda phage expression library, we identified one of these as the novel membrane protein LfhA. Ligand affinity assays and surface plasmon resonance analyses of recombinant LfhA revealed specific binding of both factor H and factor H-related protein 1. Serological examination of infected humans and horses demonstrated that LfhA is expressed by L. interrogans during mammalian infection. LfhA may therefore contribute to the resistance of pathogenic leptospires to complement-mediated killing during leptospiremic phases of the disease.
钩端螺旋体感染的早期阶段特征是血液中存在活的病原体。致病性问号钩端螺旋体对补体介导杀伤的替代途径具有抗性,而该属的非致病性成员则不具有抗性。与该观察结果一致的是,只有致病性钩端螺旋体结合因子H,它是替代补体途径的一种宿主液相调节剂。配体亲和印迹分析表明,致病性问号钩端螺旋体产生至少两种因子H结合蛋白。通过筛选λ噬菌体表达文库,我们鉴定出其中一种为新型膜蛋白LfhA。重组LfhA的配体亲和测定和表面等离子体共振分析显示因子H和因子H相关蛋白1均有特异性结合。对受感染的人类和马匹进行的血清学检查表明,LfhA在哺乳动物感染期间由问号钩端螺旋体表达。因此,LfhA可能有助于致病性钩端螺旋体在疾病的钩端螺旋体血症阶段抵抗补体介导的杀伤作用。